Determination of Fluoride in Antarctic Krill Euphausia superba Using Ion Chromatography

A simple, rapid and accurate method for the determination of fluoride in Antarctic krill has been developed. The fluoride content in Antarctic krill was determined by ion chromatography. The method requires a simple sample clean-up procedure to remove the interfering Cl- from the hydrochloric acid extraction solution. The optimum extraction conditions of fluoride from Antarctic krill samples were obtained by adding 8mL of 1:11(v/v) hydrochloric acid solution and extracting for 60 min. Under these conditions, recoveries of fluoride from Euphausia superba and Penaeus vannamei were 97.9-105.6% and 95.1-101.9%, respectively. The limit of detection was 0.01mg/kg. The method was applied to the determination of fluoride in Antarctic krill. Key words: Fluoride, Antarctic krill, Ion chromatography

Fluoride sorption and mineral stability in an Alberta soil interacting with phosphogypsum leachate

A by-product of phosphate fertilizer production is phosphogypsum (PG). Relatively high F concentrations occur in the solid phase and in the highly acidic process water (PW) that initially fills its pores. The present research addresses the fate of F and the effects on mineral stability as phosphogypsum leachate (PGL) interacts with calcareous (Ck) soil and non-calcareous (Bt) soil. In a sequential batch equilibration, soils were exposed to fresh PGL during 30 d-long extractions. Major ions, pH and electrical conductivity (EC) were monitored. At 28 d, F concentration decreased from 31 mg L−1 in the PGL to 11 mg L−1 in the Bt-PGL mixture and 22 mg L−1 in the Ck-PGL mixture. Saturation indices (SIs) for fluorite ranged from 2.1 to −3.6. Extracts were closer to saturation with fluorite than with the other F minerals studied. Using alternative geochemical constants, fluorapatite was predicted to be stable in Bt-PGL extracts. The day 28 Bt-PGL extract was also near equilibrium with alunite, basaluminite, jurbanite, gypsum, amorphous silica, and quartz. Of the phyllosilicates in the soil-PGL mixtures at day 28, only kaolinite was predicted to be stable in only the Bt-PGL mixture. The potential for clay mineral instability and accelerated dissolution in F-rich PGL needs to be considered m the design of PG repositories. Key words: Fluoride, phosphogypsum, waste management, leachates, geochemical modeling, mineral stability

Response of some vegetable crops to soil-applied halides

The halide elements are environmentally important and share some common attributes. The heaviest, I, and the lighest, F, are quite toxic and are important industrial pollutants. They are also effectively retained in soils. The others, Cl and Br, can be accumulated to high concentrations in plants, are used in agriculture and are highly mobile in soils. This study investigated the behaviour of the halides in plots, outdoor lysimeters, and laboratory sorption and excised-root experiments. Sorption on soil was ordered as F > I > Br > Cl. Concentrations in plants were generally ordered as CI ≥ Br > > F ≥ I, the inverse of the sorption ordering, as expected. Older tissues, which were also closest to the soil surface, had higher concentrations, and sequestered tissues, such as corn kernels and cabbage heads, had lower concentrations. There was evidence of competitive interaction among the halides and with soil anions such as phosphate and sulfate. This competition reduced the toxicity of I and modified tissue concentrations of the halides, P and S. Another interesting interaction was an increase in Cl and I sorption on soil solids when there were elevated levels or the other halides. Overall, the study of the halides in combination enhanced our understanding of their individual behaviours. Key words: Fluoride, chloride, bromide, iodide, vegetable